W Nillesen

Benign familial hematuria due to mutation of the type IV collagen alpha4 gene.

Henny H. Lemmink, W Nillesen, Toshio Mochizuki et al. · Journal of Clinical Investigation · 1996 · 205 citations · Full text

Medicine, Genetics, Nephrology +17

Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.

Gert Jansen, Patrick J. Willems, M. Coerwinkel et al. · PubMed · 1994 · 163 citations

Life Sciences, Genetics, Molecular Genetics +15

Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).

H G Brunner, H T Brüggenwirth, W Nillesen et al. · PubMed · 1993 · 109 citations

Life Sciences, Genetics, Neurology +8

Presymptomatic diagnosis of myotonic dystrophy.

Han G. Brunner, W Nillesen, Bernard A. van Oost et al. · Journal of Medical Genetics · 1992 · 75 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Familial Angelman syndrome, with a crossover in the critical deletion region

Marcel Nelen, C.J.A.M. van der Burgt, W Nillesen et al. · American Journal of Medical Genetics · 1994 · 12 citations

Life Sciences, Genetics, Molecular Genetics +17